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基于毛细管电泳/紫外检测的双重预浓缩方法灵敏测定苯胂化合物。

Sensitive determination of phenylarsenic compounds based on a dual preconcentration method with capillary electrophoresis/UV detection.

机构信息

Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, China.

出版信息

J Chromatogr A. 2011 Jul 22;1218(29):4779-87. doi: 10.1016/j.chroma.2011.05.058. Epub 2011 May 27.

Abstract

A novel method based on off-line hollow fiber based liquid liquid liquid microextraction (HF-LLLME) combined with on-column anion selective exhaustive injection (ASEI)-capillary electrophoresis/ultraviolet (CE/UV) detection was proposed for the speciation of five phenylarsenic compounds including phenylarsonic acid (PAA), 4-aminophenylarsonic acid (4-APAA), 4-hydroxyphenylarsonic acid (4-HPAA), 4-nitrophenylarsonic acid (4-NPAA) and 3-nitro-4-hydroxyphenylarsonic acid (NHPAA) in this paper. In HF-LLLME, the target analytes were extracted from 5 mL aqueous samples (donor solution pH 2.15) through a thin phase of tributyl phosphate (TBP) inside the pores of a polypropylene hollow fiber and finally into an 18 μL 0.8 mmol/L Tris acceptor solution inside the lumen of the hollow fiber. Following HF-LLLME, the acceptor solutions were directly analyzed by ASEI-CE/UV. For ASEI, a large plug of water (91% length of total capillary) was introduced into the separation capillary before sample injection in order to prolong the sample injection time, and thus enhance the stacking efficiency. Under the optimized ASEI conditions, up to 236-fold of enrichment factor (EF) was obtained for the ASEI-CE/UV determination of target phenylarsenic compounds. By combining HF-LLLME with ASEI-CE/UV, EFs ranging from 155 to 1780-fold were achieved and the limits of detection (LODs) (at a signal-to-noise ratio of 3) were in the range of 0.68-6.90 μg/L for five phenylarsenic compounds; the relative standard deviations (RSDs) of corrected peak area were 5.6-11.8%. The proposed HF-LLLME-ASEI-CE/UV method was applied for the determination of five target phenylarsenic compounds in pig feed from a local pig farm, and storage pig litter, soil in agricultural field and lake water collected near this pig farm, the recoveries for the spiked samples were in the range of 85.7-104.5%, 66.7-96.2%, 28.9-46.9% and 86.9-107.8% for pig feed, pig litter, soil and lake water, respectively.

摘要

本文提出了一种基于离线中空纤维液液液微萃取(HF-LLLME)结合柱上进样阴离子选择完全萃取(ASEI)-毛细管电泳/紫外(CE/UV)检测的新方法,用于五种苯胂化合物的形态分析,包括苯胂酸(PAA)、4-氨基苯胂酸(4-APAA)、4-羟基苯胂酸(4-HPAA)、4-硝基苯胂酸(4-NPAA)和 3-硝基-4-羟基苯胂酸(NHPAA)。在 HF-LLLME 中,目标分析物从 5mL 水相样品(供体溶液 pH 2.15)中通过聚丙稀中空纤维孔内的薄相三丁基磷酸盐(TBP)萃取,并最终进入中空纤维内腔内的 18μL0.8mmol/L 三羟甲基氨基甲烷接受溶液中。HF-LLLME 后,采用 ASEI-CE/UV 直接分析接受溶液。对于 ASEI,在样品进样前,将一大段水(总毛细管长度的 91%)引入分离毛细管中,以延长样品进样时间,从而提高堆积效率。在优化的 ASEI 条件下,目标苯胂化合物的 ASEI-CE/UV 测定得到了高达 236 倍的富集因子(EF)。通过将 HF-LLLME 与 ASEI-CE/UV 相结合,可实现 155 至 1780 倍的 EF,并可获得五种苯胂化合物的检测限(LOD)(信噪比为 3)在 0.68-6.90μg/L 范围内;经修正的峰面积相对标准偏差(RSD)为 5.6-11.8%。该方法已应用于当地养猪场猪饲料、储存猪粪、农田土壤和养猪场附近湖泊水中五种目标苯胂化合物的测定,加标样品的回收率在猪饲料、猪粪、土壤和湖水的回收率分别为 85.7-104.5%、66.7-96.2%、28.9-46.9%和 86.9-107.8%。

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